| Product NDC: | 55154-9441 |
| Proprietary Name: | POTASSIUM CHLORIDE |
| Non Proprietary Name: | POTASSIUM CHLORIDE |
| Active Ingredient(s): | 1.5 g/15mL & nbsp; POTASSIUM CHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55154-9441 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19690101 |
| Package NDC: | 55154-9441-5 |
| Package Description: | 5 CUP, UNIT-DOSE in 1 BAG (55154-9441-5) > 30 mL in 1 CUP, UNIT-DOSE |
| NDC Code | 55154-9441-5 |
| Proprietary Name | POTASSIUM CHLORIDE |
| Package Description | 5 CUP, UNIT-DOSE in 1 BAG (55154-9441-5) > 30 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 55154-9441 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POTASSIUM CHLORIDE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19690101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 1.5 |
| Strength Unit | g/15mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |